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首页|期刊导航|四川大学学报(医学版)|DNA损伤修复基因XRCC4、RAD51单核苷酸多态性与中国地区食管癌易感相关性研究

DNA损伤修复基因XRCC4、RAD51单核苷酸多态性与中国地区食管癌易感相关性研究

范雪娇 任朋亮 卢钟娇 赵书 杨晓龙 刘戟

四川大学学报(医学版)2013,Vol.44Issue(4):568-572,5.
四川大学学报(医学版)2013,Vol.44Issue(4):568-572,5.

DNA损伤修复基因XRCC4、RAD51单核苷酸多态性与中国地区食管癌易感相关性研究

The Study of Esophageal Cancer Risk Associated with Polymorphisms of DNA Damage Repair Genes XRCC4 and RAD51

范雪娇 1任朋亮 1卢钟娇 1赵书 1杨晓龙 1刘戟1

作者信息

  • 1. 四川大学华西基础医学与法医学院生物化学与分子生物学教研室 成都 610041
  • 折叠

摘要

Abstract

Objective Investigate the association between genetic polymorphism of DSBs repair gene XRCC4,RAD51 and susceptibility to esophageal cancer (EC).Methods A hospital based case-control study with 123 EC cases and 61 controls in a Chinese population was conducted.PCR-RFLP was applied to investigate the genotype of XRCC4 promoter G-1394T (rs6869366) and RAD51-G135C and then statistical analysis was conducted by calculating the adjusted odds ratios (OR) and 95% confidence intervals (95%CI).Results A significant difference of XRCC4-1394 polymorphism was observed between EC cases and controls (P<0.05).Carriers of the XRCC4 rs6869366 G allele (GC+GG) were at a higher risk of developing EC with the TT genotype as reference (OR=3.022,95%CI=1.487-6.142,P=0.002).When GG served as the reference group of RAD51-G135C allele,variant genotype (GC and CC) had a significant increased risk of lung cancer (OR=3.643,95 %CI=1.501-8.842,P<0.05).Conclsion Our findings indicated that genetic variants in DNA repair pathways may be involved in esophageal tumorigenesis.XRCC4 G-1394T and RAD51-G135C conferred risk for the process of developing EC.

关键词

XRCC4/RAD51/食管癌/单核苷酸多态性

Key words

XRCC4/RAD51/Esophageal cancer/Single nucleotide polymorphism

引用本文复制引用

范雪娇,任朋亮,卢钟娇,赵书,杨晓龙,刘戟..DNA损伤修复基因XRCC4、RAD51单核苷酸多态性与中国地区食管癌易感相关性研究[J].四川大学学报(医学版),2013,44(4):568-572,5.

基金项目

教育部博士点基金新教师项目(No.20070610124)和教育部留学回国人员启动基金项目(No.2008890-19-11)资助 (No.20070610124)

四川大学学报(医学版)

OA北大核心CSCDCSTPCDMEDLINE

1672-173X

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